Expression of the ELAV-like protein HuR is associated with higher tumor grade and increased cyclooxygenase-2 expression in human breast carcinoma

被引:135
作者
Denkert, C
Weichert, W
Winzer, KJ
Müller, BM
Noske, A
Niesporek, S
Kristiansen, G
Guski, H
Dietel, M
Hauptmann, S
机构
[1] Charite Hosp, Inst Pathol, D-10117 Berlin, Germany
[2] Charite Hosp, Inst Breast Canc, D-10117 Berlin, Germany
[3] Univ Halle Wittenberg, Inst Pathol, Halle An Der Saale, Saale, Germany
关键词
D O I
10.1158/1078-0432.CCR-04-0070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The human ELAV (embryonic lethal abnormal vision)-like protein HuR stabilizes a certain group of cellular mRNAs that contain AU-rich elements in their 3'-untranslated region. Cell culture studies have shown that the mRNA of cyclooxygenase (COX)-2 can be stabilized by HuR. Experimental Design: To investigate a possible contribution of dysregulation of mRNA stability to the progression of cancer and to overexpression of COX-2, we studied expression of HuR in 208 primary breast carcinomas by immunohistochemistry. Results: There were two different staining patterns of HuR in tumor tissue of breast carcinomas: nuclear expression was seen in 61 % of cases; and an additional cytoplasmic expression was seen in 30 % of cases. Expression of HuR was significantly associated with increased COX-2 expression; this association was particularly significant for cytoplasmic HuR expression (P < 0.0005). We further observed a significant association of cytoplasmic (P = 0.002) or nuclear HuR (P = 0.027) expression with increased tumor grade. Only 13% of the grade 1 carcinomas showed cytoplasmic expression of HuR, compared with 46% of the grade 3 carcinomas. There was no significant correlation between HuR expression and other clinicopathological parameters such as histological type, tumor size, or nodal status as well as patient survival. Conclusions: Our results suggest that overexpression of HuR in tumor tissue may be part of a regulatory pathway that controls the mRNA stability of several important targets in tumor biology, such as COX-2. Based on our results, additional studies are necessary to investigate whether HuR might be a potential target for molecular tumor therapy.
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页码:5580 / 5586
页数:7
相关论文
共 29 条
[1]   Cyclooxygenase inhibition in cancer prevention and treatment [J].
Anderson, WF ;
Umar, A ;
Hawk, ET .
EXPERT OPINION ON PHARMACOTHERAPY, 2003, 4 (12) :2193-2204
[2]  
Atasoy U, 1998, J CELL SCI, V111, P3145
[3]   Protein ligands to HuR modulate its interaction with target mRNAs in vivo [J].
Brennan, CM ;
Gallouzi, IE ;
Steitz, JA .
JOURNAL OF CELL BIOLOGY, 2000, 151 (01) :1-13
[4]   Role of the RNA-binding protein HuR in colon carcinogenesis [J].
de Silanes, IL ;
Fan, JS ;
Yang, XL ;
Zonderman, AB ;
Potapova, O ;
Pizer, ES ;
Gorospe, M .
ONCOGENE, 2003, 22 (46) :7146-7154
[5]   Elevated expression of cyclooxygenase-2 is a negative prognostic factor for disease free survival and overall survival in patients with breast carcinoma [J].
Denkert, C ;
Winzer, KJ ;
Müller, BM ;
Weichert, W ;
Pest, S ;
Köbel, M ;
Kristiansen, G ;
Reles, A ;
Siegert, A ;
Guski, H ;
Hauptmann, S .
CANCER, 2003, 97 (12) :2978-2987
[6]   Overexpression of the embryonic-lethal abnormal vision-like protein HuR in ovarian carcinoma is a prognostic factor and is associated with increased cyclooxygenase 2 expression [J].
Denkert, C ;
Weichert, W ;
Pest, S ;
Koch, I ;
Licht, D ;
Köbel, M ;
Reles, A ;
Sehouli, J ;
Dietel, M ;
Hauptmann, S .
CANCER RESEARCH, 2004, 64 (01) :189-195
[7]  
Dixon DA, 2003, PROG EXP TUMOR RES, V37, P52
[8]   Altered expression of the mRNA stability factor HuR promotes cyclooxygenase-2 expression in colon cancer cells [J].
Dixon, DA ;
Tolley, ND ;
King, PH ;
Nabors, LB ;
McIntyre, TM ;
Zimmerman, GA ;
Prescott, SM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (11) :1657-1665
[9]  
Eifel P, 2001, JNCI-J NATL CANCER I, V93, P979
[10]   PATHOLOGICAL PROGNOSTIC FACTORS IN BREAST-CANCER .1. THE VALUE OF HISTOLOGICAL GRADE IN BREAST-CANCER - EXPERIENCE FROM A LARGE STUDY WITH LONG-TERM FOLLOW-UP [J].
ELSTON, CW ;
ELLIS, IO .
HISTOPATHOLOGY, 1991, 19 (05) :403-410